510(k) K904500

ELASTOPLAST by Beiersdorf, Inc. — Product Code KGX

K904500 is an FDA 510(k) premarket notification submitted by Beiersdorf, Inc. for the device "ELASTOPLAST". The FDA issued a decision of Substantially Equivalent on November 21, 1990. The device falls under product code KGX (Tape And Bandage, Adhesive), a Class I device regulated under 21 CFR 880.5240. Beiersdorf, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 21, 1990
Date Received
October 2, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tape And Bandage, Adhesive
Device Class
Class I
Regulation Number
880.5240
Review Panel
SU
Submission Type